Biology subjects

Redmond, A. K.

Publications and source records attributed to Redmond, A. K..

5 recordsLinked to original sources

bioRxiv2026

Cryptic whole-genome duplication in bryozoans

Whole-genome duplications (WGDs) have long been proposed as evolutionary facilitators of biological complexity and diversification. Ancient WGDs occurred deep in the evolutionary history of both plants and vertebrates, but appear to be rare in invertebrates. However, it is unclear whether this reflects genuine scarcity or inadequate detection methodologies, and current methods may be insufficient to detect very old WGDs where extensive gene loss has followed. Here, we used a combination of paralogous and orthologous synteny-based methods incorporating bilaterian ancestral linkage groups (ALGs) to search for genomic signatures of WGD in members of the invertebrate phylum Bryozoa. This revealed strong evidence for an ancient WGD in the freshwater bryozoan Cristatella mucedo, Class Phylactolaemata, with duplicated paralogous regions across every chromosome. Only ~10% of duplicated genes are retained, including a Hox cluster duplication. All eight genomes from the bryozoan class Gymnolaemata also show signatures of ancient WGD in the form of 2:1 ratios in orthologous synteny comparisons, which remain detectable despite only ~5% duplicate retention. Gene trees support a scenario in which all extant bryozoans share an ancient WGD and much of the genome rediploidised independently in the two clades. Duplicates retained after bryozoan WGD are enriched in cilia genes and are preferentially expressed in the lophophore, the tentacular feeding organ covered in highly specialised cilia. We argue that cryptic WGD in bryozoan evolution facilitated adaptation to a sessile, filter-feeding lifestyle, and propose that incorporation of ALGs adds to the power of synteny-based WGD-detection methods.

genomics↗

bioRxiv2026

A Duplicate Resolved Paddlefish Genome Provides Insights into the Mechanisms of Rediploidisation and Hox Cluster Evolution

Whole-genome duplication (WGD; or polyploidy) has played a major role in the evolution of many lineages however, our understanding of the processes that shape genome evolution following WGD remains incomplete. While polyploidy duplicates the entire genome sequence, it is rediploidisation that establishes independent duplicated genes. Rediploidisation proceeds through suppression of meiotic recombination across polysomic loci thus restoring disomic inheritance, a process that is not synchronised across the genome. Despite its importance, the mechanisms underlying this process remain poorly understood. The slowly evolving genomes of paleopolyploid Acipenseriformes paddlefish and sturgeon provide an invaluable system for investigating this, as rediploidisation was highly asynchronous in these lineages. In both genomes ohnologs tend to segregate into blocks on the chromosomes according to rediploidisation timing, a pattern that suggests links between chromosomal structure and rediploidisation. Here, we analyse a newly-produced duplicate-resolved paddlefish genome assembly and show a strong concordance between genome rearrangement and rediploidisation timing. We also find that topologically associated domain (TAD) boundaries are associated with rediploidisation block boundaries. Together these results indicate that rediploidisation in acipenseriformes occurred through a process of genome rearrangements that was subject to functional constraints imposed by 3D genome architecture. We investigate the evolution of Hox clusters in these lineages, revealing a previously overlooked duplicate HoxC region in paddlefish, and both ancestral and lineage-specific Hox cluster rediploidisation with substantially different timings. These findings highlight a complex evolutionary history following WGD in Acipenseriformes with implications for understanding short-term adaptations to polyploidy as well as longer-term diversification of lineages.

evolutionary biology↗

bioRxiv2026

An automated pipeline for reconstructing whole genome duplications

Whole genome duplications leave lasting traces in our genomes. How these present in terms of gene content and order varies over time. While collinear blocks of paralogs, long stretches of conserved gene order and content termed microsynteny, are a distinctive feature of comparatively recent WGD and have been integral in reconstructing the history of ancestral duplication events, this signal degrades over time, making analysis of older events non-trivial. While gene order degrades quickly, gene content is often better conserved and recent work takes advantage of this to reconstruct older events and ancestral pre-WGD and post-WGD chromosomes. However, these new methods are complicated and not well-documented. Here we develop an automated and user-friendly pipeline for reconstructing ancestral chromosomes before and after WGD, and use the conservation of gene content to infer chromosomal rearrangement events in this timeframe. We verify the efficacy of our tool by reconstructing the ancestral acipenseriform, a model system for vertebrate WGD and rediploidisation. Our pipeline should serve to make ancestral reconstruction more accessible and provide a solid foundation for future analysis.

evolutionary biology↗

bioRxiv2023

Acoelomorph flatworm monophyly is a severe long-branch attraction artefact obscuring a clade of Acoela and Xenoturbellida

Acoelomorpha is a broadly accepted clade of bilaterian animals made up of the fast-evolving, morphologically simple, mainly marine flatworm lineages Acoela and Nemertodermatida. Phylogenomic studies support Acoelomorphas close relationship with the slowly evolving and similarly simplistic Xenoturbella, together forming the phylum Xenacoelomorpha. The phylogenetic placement of Xenacoelomorpha amongst bilaterians is controversial, with some studies supporting Xenacoelomorpha as the sister group to all other bilaterians, implying that their simplicity may be representative of early bilaterians. Others propose that this placement is a long branch attraction artefact resulting from the fast-evolving Acoelomorpha, and instead suggest that they are the secondarily simplified sister group of the deuterostome clade Ambulacraria. Perhaps as a result of this debate, internal xenacoelomorph relationships have been somewhat overlooked at a phylogenomic scale. Here, I employ both empirical and simulation approaches to detect and overcome phylogenomic errors to reassess the relationship between Xenoturbella and the fast evolving acoelomorph flatworms. I conclude that subphylum Acoelomorpha is a long-branch attraction artefact obscuring a previously undiscovered clade comprising Xenoturbella and Acoela, for which I propose the name Xenacoela. These analyses are also consistent with the Nephrozoa hypothesis deriving from systematic error, and instead generally favour a close, but unclear, relationship of Xenacoelomorpha with deuterostomes. This study provides a template for future efforts aimed at discovering and correcting unrecognised long-branch attraction artefacts throughout the tree of life.

evolutionary biology↗

bioRxiv2022

Extensive lineage-specific rediploidisation masks shared whole genome duplication in the sturgeon-paddlefish ancestor

Whole genome duplication (WGD) is a dramatic evolutionary event generating many new genes and which may play a role in survival through mass extinctions. Paddlefish and sturgeon are sister lineages that both show genomic evidence for ancient WGD. Until now this has been interpreted as two independent WGD events due to a preponderance of duplicate genes with independent histories. Here we show that although there is indeed a plurality of apparently independent gene duplications, these derive from a shared genome duplication event occurring close to the Permian-Triassic mass extinction period, followed by a prolonged process of reversion to stable diploid inheritance (rediploidisation). We show that the sharing of this WGD is masked by the fact that paddlefish and sturgeon lineage divergence occurred before rediploidisation had proceeded even half-way. Thus, for most genes the resolution to diploidy was lineage-specific. Because genes are only truly duplicated once diploid inheritance is established, the paddlefish and sturgeon genomes are a mosaic of shared and non-shared gene duplications resulting from a shared genome duplication event. This is the first time that lineage-specific resolution of genes from a common WGD event has been shown to affect such a large proportion of the genome.

evolutionary biology↗